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David R Beier

Showing results (41-50 of 88) with videos related to

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Development (Cambridge, England)|November 8, 2002
A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafishShanming Liu, Weining Lu, Tomoko Obara, et al.
The Journal of Comparative Neurology|July 24, 2012
Mutation of the BiP/GRP78 gene causes axon outgrowth and fasciculation defects in the thalamocortical connections of the mammalian forebrainCarlita B Favero, Rasha N Henshaw, Cynthia M Grimsley-Myers, et al.
The Journal of Biological Chemistry|May 12, 2011
Lipoxygenases mediate the effect of essential fatty acid in skin barrier formation: a proposed role in releasing omega-hydroxyceramide for construction of the corneocyte lipid envelopeYuxiang Zheng, Huiyong Yin, William E Boeglin, et al.
Plos One|December 11, 2012
A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosisJianning Tao, Maranke I Koster, Wilbur Harrison, et al.
Molecular Biology and Evolution|April 21, 2019
Applicability of the Mutation-Selection Balance Model to Population Genetics of Heterozygous Protein-Truncating Variants in HumansDonate Weghorn, Daniel J Balick, Christopher Cassa, et al.
The Journal of Investigative Dermatology|April 13, 2007
A mouse mutation in the 12R-lipoxygenase, Alox12b, disrupts formation of the epidermal permeability barrierJennifer L Moran, Haiyan Qiu, Annick Turbe-Doan, et al.
Plos Genetics|September 14, 2011
Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivoRolf W Stottmann, Annick Turbe-Doan, Pamela Tran, et al.
Molecular and Cellular Biology|September 7, 2002
Gene structure and functional analysis of the mouse nidogen-2 gene: nidogen-2 is not essential for basement membrane formation in miceJürgen Schymeinsky, Sabine Nedbal, Nicolai Miosge, et al.
The Journal of Clinical Investigation|February 21, 2002
Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney diseaseXiaoying Hou, Michal Mrug, Bradley K Yoder, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 2, 2009
Concurrent Lpin1 and Nrcam mouse mutations result in severe peripheral neuropathy with transitory hindlimb paralysisDarlene S Douglas, Jennifer L Moran, John R Bermingham, et al.
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
Development (Cambridge, England)|November 8, 2002
A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafishShanming Liu, Weining Lu, Tomoko Obara, et al.
The Journal of Comparative Neurology|July 24, 2012
Mutation of the BiP/GRP78 gene causes axon outgrowth and fasciculation defects in the thalamocortical connections of the mammalian forebrainCarlita B Favero, Rasha N Henshaw, Cynthia M Grimsley-Myers, et al.
The Journal of Biological Chemistry|May 12, 2011
Lipoxygenases mediate the effect of essential fatty acid in skin barrier formation: a proposed role in releasing omega-hydroxyceramide for construction of the corneocyte lipid envelopeYuxiang Zheng, Huiyong Yin, William E Boeglin, et al.
Plos One|December 11, 2012
A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosisJianning Tao, Maranke I Koster, Wilbur Harrison, et al.
Molecular Biology and Evolution|April 21, 2019
Applicability of the Mutation-Selection Balance Model to Population Genetics of Heterozygous Protein-Truncating Variants in HumansDonate Weghorn, Daniel J Balick, Christopher Cassa, et al.
The Journal of Investigative Dermatology|April 13, 2007
A mouse mutation in the 12R-lipoxygenase, Alox12b, disrupts formation of the epidermal permeability barrierJennifer L Moran, Haiyan Qiu, Annick Turbe-Doan, et al.
Plos Genetics|September 14, 2011
Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivoRolf W Stottmann, Annick Turbe-Doan, Pamela Tran, et al.
Molecular and Cellular Biology|September 7, 2002
Gene structure and functional analysis of the mouse nidogen-2 gene: nidogen-2 is not essential for basement membrane formation in miceJürgen Schymeinsky, Sabine Nedbal, Nicolai Miosge, et al.
The Journal of Clinical Investigation|February 21, 2002
Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney diseaseXiaoying Hou, Michal Mrug, Bradley K Yoder, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 2, 2009
Concurrent Lpin1 and Nrcam mouse mutations result in severe peripheral neuropathy with transitory hindlimb paralysisDarlene S Douglas, Jennifer L Moran, John R Bermingham, et al.
Pageof 9